27 results
·
27ms
·
Sources: EU EUDAMED, US FDA
STANDARD IMAGING IVB 1000 WELL CHAMBER
FDA 510(k)
FDA Class 2
·Radiology
ACUFEX
FDA UDI
Smith & Nephew, Inc.·03596010024954·12 MM CANNULATED DRILL BIT
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450582329·
Gaudi
FDA UDI
NETBIOLOGICS, LLC·G682G0135481·Fixation Screw, for Gaudi Plate, OD=3.5mm, LEN=...
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·December 16, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·December 16, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·December 16, 2025
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033512623·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033512654·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033512647·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033512616·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033512630·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033512609·
Phantom® Fibula Nail System
FDA UDI
Paragon 28, Inc.·00889795134233·3.5mm x 48mm, Threaded Peg, Ti
MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)
FDA 510(k)
FDA Class 2
·Neurology
PADPRO SYSTEM DEFIBRILLATOR ELECTRODE ADAPTERS
FDA 510(k)
FDA Class 3
·Cardiovascular
ACCU-CHEK ® SMARTVIEW TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·December 27, 2013
ACCU-CHEK ® SMARTVIEW TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·December 27, 2013
BD VIPER¿ LT SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·June 15, 2023
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 20, 2013